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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1889010Generated: November 1, 2026

Triethylamine → 4-[(3-Chloro-4-fluoro-2-methylphenyl)carbonyl]-2-piperazinone

https://huagongshe.com/reaction/1889010

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPiperazin-2-oneHCID 231360—
Reactant3-Chloro-4-fluoro-2-methylbenzoyl chlorideHCID 86666739—
SolventDichloromethaneHCID 6344—
Product4-[(3-Chloro-4-fluoro-2-methylphenyl)carbonyl]-2-piperazinoneHCID 66599262—

Reaction Steps

2-piperazinone (0.350 g, 3.5 mmol, commercially available from e.g. Sigma-Aldrich) was dissolved in dichloromethane (DCM) (15 mL), and to this was added triethylamine (0.585 mL, 4.20 mmol). The solution was then cooled to 0° C. before 3-chloro-4-fluoro-2-methylbenzoyl chloride (I58) (0.797 g, 3.85 mmol) in Dichloromethane (DCM) (5 mL) was added dropwise. The solution was stirred, under argon, for 30 minutes before the solvent was evaporated in vacuo. The remaining residue was then re-dissolved in DCM (50 mL) and washed with water (20 mL), a saturated solution of sodium bicarbonate (20 mL) and brine (20 mL). The organic phase was then dried over anhydrous sodium sulphate, which was then filtered off and the solvent was evaporated in vacuo. The remaining solid was then stirred in hexane (30 mL) at 55° C. for 30 minutes, before being filtered to yield the product in 0.843 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501946B2
Source datasetuspto-grants-2013_08
ORD IDord-5289b1b5414349dfa137415ef4d2b324
Source noteuspto-grants-2013_08